MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. EVOLUTIONMP FEM CS/CR NON-POR SIZE 7 PRIMARY LEFT; KNEE COMPONENT

Model Number EFSRN7PL

Device Problem Appropriate Term/Code Not Available (3191)

Patient Problem Unspecified Infection (1930)

Event Type  Injury  

Manufacturer Narrative

This event will be updated once the investigation is complete.Trends will be evaluated.

Event Description

Allegedly, patient revised due to knee infection.No further information could be obtained and this was already reported and investigated by (b)(4), reference (b)(4).

• Brand Name: EVOLUTIONMP FEM CS/CR NON-POR SIZE 7 PRIMARY LEFT
• Type of Device: KNEE COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer (Section G): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer Contact: 5677 airline road; arlington, TN 38002 ; 9018674771
• MDR Report Key: 11586334
• MDR Text Key: 242883777
• Report Number: 3010536692-2021-00184
• Device Sequence Number: 1
• Product Code: HRY
• UDI-Device Identifier: M684EFSRN7PL1
• UDI-Public: M684EFSRN7PL1
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: K093552
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 05/28/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Other
• Device Model Number: EFSRN7PL
• Device Catalogue Number: EFSRN7PL
• Device Lot Number: 1453918
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 03/15/2021
• Initial Date Manufacturer Received: 03/15/2021
• Initial Date FDA Received: 03/29/2021
• Supplement Dates Manufacturer Received: 03/15/2021
• Supplement Dates FDA Received: 05/28/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention